Last updated: May 20, 2022
Sponsor: Istanbul University
Overall Status: Active - Recruiting
Phase
N/A
Condition
Enuresis
Urinary Incontinence
Interstitial Cystitis
Treatment
N/AClinical Study ID
NCT05391425
solifenacinpm
Ages 18-90 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Women presented in Arnavutkoy State Hospital Gynecology Clinic with lower urinarytract symptoms that are planned to start treatment with Solifenacin 5 mg (Vesicare 5mg).
- Patients agreed to involve in the study, having discussed other treatment options andpossible side effects of the medication.
- Informed consent obtained
Exclusion
Exclusion Criteria:
- urinary tract infection
- stress urinary incontinence
- urinary retention
- grade 2 or above pelvic organ prolapse according to POP-Q scale
- Solifenacin contraindications such as narrow angle glaucoma, allergy of Solifenacin orother components of the drug.
Study Design
Total Participants: 150
Study Start date:
June 03, 2021
Estimated Completion Date:
June 03, 2024
Study Description
Connect with a study center
Arnavutkoy State Hospital
Istanbul, Arnavutkoy 34275
TurkeyActive - Recruiting

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